Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5509855 | Clinica Chimica Acta | 2016 | 7 Pages |
Abstract
Results suggested that the NGS approach based on AmpliSeq⢠libraries and Ion PGM sequencing is a highly efficient mutation detection method. It is suitable for large-scale sequencing of opioid receptor genes. The method includes the variants studied so far for functional associations and adds a large amount of genetic information as a basis for complete analysis of human opioid receptor genetics and its functional consequences.
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Authors
Dario Kringel, Jörn Lötsch,